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内质网相关蛋白降解中新型A1PiZ降解缺陷(ADD)基因的差异需求。

Differential requirements of novel A1PiZ degradation deficient (ADD) genes in ER-associated protein degradation.

作者信息

Palmer Elizabeth A, Kruse Kristina B, Fewell Sheara W, Buchanan Sean M, Brodsky Jeffrey L, McCracken Ardythe A

机构信息

Biology Department, University of Nevada, Reno, NV 89557, USA.

出版信息

J Cell Sci. 2003 Jun 1;116(Pt 11):2361-73. doi: 10.1242/jcs.00439. Epub 2003 Apr 23.

Abstract

In the eukaryotic cell, a protein quality control process termed endoplasmic reticulum-associated degradation (ERAD) rids the ER of aberrant proteins and unassembled components of protein complexes that fail to reach a transport-competent state. To identify novel genes required for ERAD, we devised a rapid immunoassay to screen yeast lacking uncharacterized open reading frames that were known targets of the unfolded protein response (UPR), a cellular response that is induced when aberrant proteins accumulate in the ER. Six genes required for the efficient degradation of the Z variant of the alpha1-proteinase inhibitor (A1PiZ), a known substrate for ERAD, were identified, and analysis of other ERAD substrates in the six A1PiZ-degradation-deficient (add) mutants suggested diverse requirements for the Add proteins in ERAD. Finally, we report on bioinformatic analyses of the new Add proteins, which will lead to testable models to elucidate their activities.

摘要

在真核细胞中,一种称为内质网相关降解(ERAD)的蛋白质质量控制过程可清除内质网中的异常蛋白质以及未能达到转运能力状态的蛋白质复合物未组装成分。为了鉴定ERAD所需的新基因,我们设计了一种快速免疫测定法,以筛选缺乏未表征开放阅读框的酵母,这些开放阅读框是未折叠蛋白反应(UPR)的已知靶点,UPR是一种当异常蛋白质在内质网中积累时诱导的细胞反应。我们鉴定出了高效降解α1-蛋白酶抑制剂Z变体(A1PiZ)(一种已知的ERAD底物)所需的六个基因,并且对六个A1PiZ降解缺陷(add)突变体中的其他ERAD底物进行分析表明,Add蛋白在ERAD中有多种需求。最后,我们报告了对新Add蛋白的生物信息学分析,这将有助于建立可测试的模型以阐明它们的活性。

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